Canonical Allele Identifier: CA1076343133

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1748206644
• gnomAD v3: 5-56881555-G-GC
• gnomAD v4: 5-56881555-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881555_56881556insC , CM000667.2:g.56881555_56881556insC	GRCh38
NC_000005.9:g.56177382_56177383insC , CM000667.1:g.56177382_56177383insC	GRCh37
NC_000005.8:g.56213139_56213140insC	NCBI36
NG_031884.1:g.71483_71484insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.2370-15_2370-14insC MANE Select	ENSP00000382423.3:n.2370-15_2370-14insC
ENST00000399503.3:c.2370-15_2370-14insC	ENSP00000382423.3:n.2370-15_2370-14insC
NM_005921.1:c.2370-15_2370-14insC	NP_005912.1:n.2370-15_2370-14insC
XM_005248519.3:c.1992-15_1992-14insC	XP_005248576.2:n.1992-15_1992-14insC
XM_011543406.1:c.2115-15_2115-14insC	XP_011541708.1:n.2115-15_2115-14insC
XM_011543407.1:c.2091-15_2091-14insC	XP_011541709.1:n.2091-15_2091-14insC
XM_011543408.1:c.2370-15_2370-14insC	XP_011541710.1:n.2370-15_2370-14insC
XM_017009484.1:c.1959-15_1959-14insC	XP_016864973.1:n.1959-15_1959-14insC
XM_017009485.1:c.1881-15_1881-14insC	XP_016864974.1:n.1881-15_1881-14insC
XR_001742068.2:n.2401-15_2401-14insC
NM_005921.2:c.2370-15_2370-14insC MANE Select	NP_005912.1:n.2370-15_2370-14insC